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    • 4 hours, 39 minutes ago
      Amy Schneider likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 6 hours, 6 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I want a thumbs down icon!
    • 6 hours, 6 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 6 hours, 6 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      When I come up with a question between visits, I usually just do some research.
    • 8 hours, 19 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 8 hours, 20 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Sorry. Of course I store unopened in frig. Opened in my room as I use it up in 30 days
    • 8 hours, 20 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      No, I keep it in the oven! ;) Same answer as the last time they asked this ridiculous question!
    • 9 hours, 2 minutes ago
      Becky Hertz likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 10 hours, 25 minutes ago
      Bruce Schnitzler likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 12 hours, 23 minutes ago
      alex likes your comment at
      Here’s What You Need to Know About the Dexcom G7
      This article explains the Dexcom G7 features in a clear and easy way, especially for people new to continuous glucose monitoring. Very informative and helpful. Sportzfy TV Download
    • 1 day, 3 hours ago
      KarenM6 likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 1 day, 3 hours ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 1 day, 3 hours ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 1 day, 3 hours ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Lol hell when haven't they. Lol
    • 1 day, 3 hours ago
      KarenM6 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 5 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was only 2 when Diagnosed 70 years ago. My small town doctor admitted he didn't know much about T1D, and fortune for my parents and I he called what is now Joslin Clinic, and they told him how much insulin to give me. He taught my parents, who then traveled over 350 miles to Boston, to learn about how to manage T1D. My doctor learned more about T1D, and was able to help 2 other young men, that were later DX with T1D in our small town. I went to Joslin until I turned 18 and returned to become a Joslin Medalist and participated in the research study, 20 years ago. Still go there for some care.
    • 1 day, 5 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was 7 when things changed in my home. My older brother was hospitalized for 2 weeks. When he came home, we no longer ate the way we had before. This was 1956. Dessert alternated between sugarless pudding or sugarless Jello. I learned that bread and potatoes had carbohydrates and that turned to sugar. There was a jar in the bathroom. It seemed my brother was testing his urine every time he went in there. There was a burner and pot on the stove designated for boiling syringes. I watched my brother give himself shots and I remember how hard it was to find someone to manage his care if my parents had to travel. Diabetic Forecast magazine came in the mail each month and there were meetings of the local diabetes association that my mother attended religiously. My brother got a kidney and pancreas transplant at age 60 and before he died lived for 5 years as a non-diabetic. A few years later I was diagnosed. Sorry he was not able to make use of today’s technology. I often wonder what he and my late parents would think about me, at age 66, being the only one in the family with type 1.
    • 1 day, 5 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 9 hours ago
      kilupx likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      My brother was type 1 since an early age. I was only diagnosed in my late 40s
    • 1 day, 11 hours ago
      Phyllis Biederman likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 12 hours ago
      Bill Williams likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was diagnosed in 1976 at the age of 18 while in college. One weekend, I was drinking a lot of water and peeing frequently. I remembered having read a Reader's Digest article on diabetes, and I told my friends I thought I might have it. Two days later, the diagnosis was confirmed.
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      It was 35 years ago for me. I had no experience with T1d. I was starting to show symptoms and my sister-in-law quickly researched T1d and told me what she found. I went to my GP a week or two later. My BG was over 600. He sent me to the hospital right away. Blood test confirmed it.
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    If you use an insulin pump, which of the following factors best describe when you will get a new pump (assuming your current pump still works)? Select all that apply!

    Home > LC Polls > If you use an insulin pump, which of the following factors best describe when you will get a new pump (assuming your current pump still works)? Select all that apply!
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    Living with T1D can be difficult, but many folks experience positives living with T1D too! No matter how small, is there anything you're grateful for related to T1D this year? Select all the options you're grateful for or share more about your experiences in the comments!

    Sarah Howard

    Sarah Howard has worked in the diabetes research field ever since she was diagnosed with T1D while in college in May 2013. Since then, she has worked for various diabetes organizations, focusing on research, advocacy, and community-building efforts for people with T1D and their loved ones. Sarah is currently the Senior Marketing Manager at T1D Exchange.

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    20 Comments

    1. Lawrence S.

      It’s all about insurance coverage for me. I’m on Medicare, so I believe it’s 5 years. It’ll be a while.

      3
      3 years ago Log in to Reply
      1. Annie Wall

        You’re right, 5 years it is, despite only having a four year warrantee.

        4
        3 years ago Log in to Reply
      2. pru barry

        We don’t really have much choice. I probably I couldn’t afford to be a diabetic without medicare, so I’m beholden to their rules and regulations. I try not to think about it all the time, but really do not like feeling trapped in a system without much input. Thinking about that makes my blood sugar rise! What’s wrong with this picture?

        1
        3 years ago Log in to Reply
    2. TomH

      When Loop or other AID is available that I can control and is NOT a black box approach. I want to know how it works and know that I control the data!

      3 years ago Log in to Reply
    3. Stephanie Cruickshank

      I’ll use my current pump until it starts acting funny and THEN I’ll get a new one. No point in replacing a perfectly good pump that I’m happy with

      3 years ago Log in to Reply
    4. ELYSSE HELLER

      My blue cross blue shield federal employee program has finally approved coverage for Omnipod 5 after months of phone calls, letters to my state senators (federal), and haggling. Great! Now that I got the Omnipod 5 I’m still waiting for an appointment with my CDE to be trained on it. I have been pumping for years but I’m not comfortable setting up this AID system by myself. If my next appointment scheduled for 12/08/2022 gets cancelled again, I will run out of the classic Omnipods and will have no choice but to figure it out on my own.

      3 years ago Log in to Reply
    5. Joan Fray

      When my CDE tells me to get one.

      3 years ago Log in to Reply
    6. Amanda Barras

      Even if a better pump comes out I have to wait out my warranty. Made it frustrating when I was stuck on a pump that wasn’t serving my needs.

      3 years ago Log in to Reply
    7. Debra Nance

      As soon as Medicare tells the supplier to ship my new pump. Waiting patiently for the call.

      3 years ago Log in to Reply
    8. Katrina Mundinger

      For years, I just upgraded my Medtronic when insurance allowed. A few months ago, just after the transmitter 1-year warranty expired, I realized how frustrated I’d been with all of the “improvements” on Medtronic’s sensors. Switched to Dexcom and because I _love_ what Auto mode had done, got help from my parents in paying the “rental” for a Tandem. So far so good!

      2
      3 years ago Log in to Reply
    9. William Bennett

      Well, my first new pump was at the end of warranty, when I “upgraded” from my old pager-style Paradigm to a Medtronic 670G. I hated the 670 so much that after about 6 months I went back to my simpler and much more reliable Paradigm, which I still had, and put the 670 back in its box, where it remains. The experience put me off the whole AID thing, to the extent that, even though I’m about two years past being eligible for a new pump, I’m really not that keen on any of the ones currently available. Yeah, I could run them on manual, but my Paradigm already does that. I have a Dexcom G6, and between the two my A1C is currently 5.8. Much better than the “automated insulin delivery” systems seem capable of delivery even now.

      3 years ago Log in to Reply
    10. Janis Senungetuk

      I can only get a new pump when allowed by Medicare, even though my primary insurance will cover a new pump every year. Medicare’s 1 year “rental” of a pump with a 4 year warranty just adds another layer of unnecessary stress.

      3 years ago Log in to Reply
    11. Marty

      I replaced my Tandem t:slim X2 pump with an identical pump when its warranty expired a couple of months ago. It was the first time in decades that I haven’t upgraded to a newer model at replacement time. I do appreciate the fact that Tandem lets me use updated software as soon as it’s available rather than having to wait for an entirely new pump. I now have a fresh warranty and a back-up pump for emergencies.

      3 years ago Log in to Reply
    12. Ceolmhor

      When the technology advances sufficiently to justify the expense and effort of making a change (probably 3-4 years).

      3 years ago Log in to Reply
    13. Mick Martin

      I would get a new pump when my Diabetes Support Team decide that I would benefit from an ‘upgrade’. (I live in the United Kingdom of Great Britain and Northern Ireland and ALL of my diabetes supplies are paid for via our NHS (National Health Service), which is financed via direct taxation of all working people.)

      3 years ago Log in to Reply
    14. Molly Jones

      1. Insurance, 2. doctors’ suggestions which probably all reflect the pumps abilities.

      3 years ago Log in to Reply
    15. csreineke

      If/when my pump stops working, I will switch to my backup. I am a DIY looper, using a compatible, older-model pump. Luckily, this means my insurance company can’t control my options. Insurance companies should not be the ones making this choice for T1D patients.

      3 years ago Log in to Reply
    16. Kayci Marr

      I will upgrade to the Omnipod 5 when I get a job with insurance…

      3 years ago Log in to Reply
    17. James Cheairs

      Am on DIY Loop – Omnipod. I see no reason to switch unless the pump I am using is no longer supported by Loop

      3 years ago Log in to Reply
    18. Tom Webb

      I use a tandem pump with basal iq and it talks with my dexcom g6 to adjust my basal as needed. It shuts my insulin off when my blood sugar goes low and asks me to treat a high both have an alert to make me aware of changes in my blood sugar.

      3 years ago Log in to Reply

    If you use an insulin pump, which of the following factors best describe when you will get a new pump (assuming your current pump still works)? Select all that apply! Cancel reply

    You must be logged in to post a comment.




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